TY - JOUR
T1 - Secondary prevention of cardiovascular disease in women
T2 - Closing the gap
AU - Thakkar, Aarti
AU - Agarwala, Anandita
AU - Michos, Erin D.
N1 - Funding Information:
EDM is supported by the Amato Fund in Women's CV Health Research at Johns Hopkins University.
Funding Information:
Disclosure: Unrelated to this work, EDM is on advisory boards for Esperion, Amarin, Novartis and Astra Zeneca. All other authors have no conflicts of interest to declare. Funding: EDM is supported by the Amato Fund in Women’s CV Health Research at Johns Hopkins University. Received: 26 May 2021 Accepted: 24 August 2021 Citation: European Cardiology Review 2021;16:e41. DOI: https://doi.org/10.15420/ecr.2021.24 Correspondence: Erin D Michos, Ciccarone Center for the Prevention of Cardiovascular Disease, Johns Hopkins University School of Medicine, Blalock 524-B, 600 N Wolfe St, Baltimore, MD 21287, US. E: edonnell@jhmi.edu Open Access: This work is open access under the CC-BY-NC 4.0 License which allows users to copy, redistribute and make derivative works for non-commercial purposes, provided the original work is cited correctly.
Publisher Copyright:
© 2021 Radcliffe Group Ltd. All rights reserved.
PY - 2021
Y1 - 2021
N2 - Cardiovascular disease (CVD) remains the leading cause of death in women globally. Younger women (<55 years of age) who experience MI are less likely to receive guideline-directed medical therapy (GDMT), have a greater likelihood of readmission and have higher rates of mortality than similarly aged men. Women have been under-represented in CVD clinical trials, which limits the generalisability of results into practice. Available evidence indicates that women derive a similar benefit as men from secondary prevention pharmacological therapies, such as statins, ezetimibe, proprotein convertase subtilisin/kexin type 9 inhibitors, icosapent ethyl, antiplatelet therapy, sodium-glucose cotransporter 2 inhibitors and glucagon-like peptide-1 receptor agonists. Women are less likely to be enrolled in cardiac rehabilitation programs than men. Mitigating risk and improving outcomes is dependent on proper identification of CVD in women, using appropriate GDMT and continuing to promote lifestyle modifications. Future research directed at advancing our understanding of CVD in women will allow us to further develop and tailor CVD guidelines appropriate by sex and to close the gap between diagnoses, treatment and mortality.
AB - Cardiovascular disease (CVD) remains the leading cause of death in women globally. Younger women (<55 years of age) who experience MI are less likely to receive guideline-directed medical therapy (GDMT), have a greater likelihood of readmission and have higher rates of mortality than similarly aged men. Women have been under-represented in CVD clinical trials, which limits the generalisability of results into practice. Available evidence indicates that women derive a similar benefit as men from secondary prevention pharmacological therapies, such as statins, ezetimibe, proprotein convertase subtilisin/kexin type 9 inhibitors, icosapent ethyl, antiplatelet therapy, sodium-glucose cotransporter 2 inhibitors and glucagon-like peptide-1 receptor agonists. Women are less likely to be enrolled in cardiac rehabilitation programs than men. Mitigating risk and improving outcomes is dependent on proper identification of CVD in women, using appropriate GDMT and continuing to promote lifestyle modifications. Future research directed at advancing our understanding of CVD in women will allow us to further develop and tailor CVD guidelines appropriate by sex and to close the gap between diagnoses, treatment and mortality.
KW - Acute MI
KW - Coronary heart disease
KW - Disparities
KW - Secondary prevention
KW - Women
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U2 - 10.15420/ecr.2021.24
DO - 10.15420/ecr.2021.24
M3 - Review article
C2 - 34815749
AN - SCOPUS:85119993183
SN - 1758-3756
VL - 16
JO - European Cardiology Review
JF - European Cardiology Review
M1 - e41
ER -